Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46780Erstellt: 23. Oktober 2026

Water → 2-(4-Phenoxyphenoxy)cyclopentan-1-ol

https://huagongshe.com/de/reaction/46780

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium borohydrideHCID 4311764—
Edukt3-(4-Phenoxyphenoxy)-cyclopenten-1-eneHCID 20385751—
KatalysatorMercuric acetateHCID 15337—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
Produkt2-(4-Phenoxyphenoxy)cyclopentan-1-olHCID 22247676—

Reaktionsschritte

A solution of 12.6 g of 3-(4-phenoxyphenoxy)-cyclopenten-1-ene in 25 ml of tetrahydrofurane is added dropwise in the course of 1 hour to a mixture of 15.9 g of mercury(II) acetate, 35 ml of water and 50 ml of tetrahydrofurane. The mixture is stirred for about 15 hours at room temperature, then 50 ml of 3 N sodium hydroxide solution are added dropwise in the course of 11/2 hours, followed by the dropwise addition in the course of 1 hour of 50 ml of a 0.5 N solution of sodium borohydride in 3 N sodium hydroxide solution. The reaction mixture is stirred for 2 hours at room temperature and precipitated mercury is removed by filtration. The filtrate is poured into ice-water and, after extraction with ether, the organic phase is washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated by rotary evaporation. Fractional distillation of the residue yields 2-(4-phenoxyphenoxy)cyclopentan-1-ol as a colourless oil with a boiling point of 181°-185° C./0.001 torr.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04175137
Quelldatensatzuspto-grants-1979_11
ORD IDord-68dcc8e1681f4418be9cbbb7c7b244ab
Quellennotizuspto-grants-1979_11